CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) - ANVISA Registration 81246982571

Access comprehensive regulatory information for CREATINE KINASE ISOENZYMES (CKMB, CKBB, CKMM) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81246982571 and manufactured by manufacturer not specified. The registration is held by ORTHO CLINICAL DIAGNÓSTICS DO BRASIL PRODUTOS PARA SAÚDE LTDA with validity until Jul 29, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, SIEMENS HEALTHCARE DIAGNOSTICS INC, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81246982571
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Registration Details
ANVISA Registration Number: 81246982571
Janaina dos Santos de Miranda

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Related Devices (2)

KIT DE REAGENTE IMUNODIAGNOSTICO VITROS* ECi PARA CK-MB
Risk Class III

Registration Details

81246982571

25351456607201748

21921393000146

Dates and Status

Aug 28, 2017

29/07/2033

09/18/2025 19:00:01

KIT DE REAGENTE IMUNODIAGNOSTICO VITROS* ECi PARA CK-MB
Risk Class III

Registration Details

81246982571

25351456607201748

21921393000146

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Aug 28, 2017

29/07/2033

09/18/2025 19:00:01